CH169242A - Process for the preparation of 5-chloro-2-acetoacetylamino-1-methoxybenzene-3-sulfonic acid. - Google Patents
Process for the preparation of 5-chloro-2-acetoacetylamino-1-methoxybenzene-3-sulfonic acid.Info
- Publication number
- CH169242A CH169242A CH169242DA CH169242A CH 169242 A CH169242 A CH 169242A CH 169242D A CH169242D A CH 169242DA CH 169242 A CH169242 A CH 169242A
- Authority
- CH
- Switzerland
- Prior art keywords
- chloro
- acetoacetylamino
- methoxybenzene
- preparation
- sulfonic acid
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von 5-Chlor-2-acetoacetylamino-l-methogybenzol-3-sulfosäure. Es wurde gefunden, dass man 5-Chlor- 2-acetoacetyl-ami n o-1- inethoxybenzol-3-s ulfo- säure dadurch erhalten kann, dass man 5-Chlor- 2-acetoacetylamino-l-methoxybenzolmit einem sulfonierenden Mittel behandelt.
<I>Beispiel:</I> 100 gr 5-Chlor-2-acetoacetylamino-l-meth- oxybeiizol werden unter Rühren bei 10 0 C in 400 gr Schwefelsäure von 20% Anhyd- ridgehalt eingetragen.
Nachdem das 5-Chlor- 2-acetoacetylamino-l-methoxybenzol gelöst ist, rührt man noch einige Zeit, bis eine mit Wasser verdünnte Probe beim Versetzen mit Natriumcarbonatlösung kein 5-Chlor-2-aceto- acetylamino -1- methogybenzol ausscheidet. Dann giesst man auf Eis und saugt die aus geschiedene 5 -Chlor- 2 - acetoacetylamino -1- methoxybenzolsulfonsäure ab.
Die neue 5- Chlor- 2 - acetoacetylamino -1- methoxybenzol- sulfonsäure bildet gut kristallisierende Alkali salze, die man aus Wasser umkristallisieren kann.
Process for the preparation of 5-chloro-2-acetoacetylamino-1-methogybenzene-3-sulfonic acid. It has been found that 5-chloro-2-acetoacetyl-amin o-1-ynethoxybenzene-3-sulfonic acid can be obtained by treating 5-chloro-2-acetoacetylamino-1-methoxybenzene with a sulfonating agent.
<I> Example: </I> 100 g of 5-chloro-2-acetoacetylamino-1-methoxybeiizole are introduced into 400 g of sulfuric acid with 20% anhydride content at 10 ° C. with stirring.
After the 5-chloro-2-acetoacetylamino-1-methoxybenzene has dissolved, stirring is continued for some time until a sample diluted with water does not separate out 5-chloro-2-acetoacetylamino -1-methogybenzene when mixed with sodium carbonate solution. It is then poured onto ice and the separated 5-chloro-2-acetoacetylamino -1-methoxybenzenesulfonic acid is filtered off with suction.
The new 5-chloro-2-acetoacetylamino -1-methoxybenzenesulfonic acid forms alkali salts which crystallize well and which can be recrystallized from water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE169242X | 1931-12-14 | ||
CH164838T | 1932-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH169242A true CH169242A (en) | 1934-05-15 |
Family
ID=25718055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH169242D CH169242A (en) | 1931-12-14 | 1932-11-15 | Process for the preparation of 5-chloro-2-acetoacetylamino-1-methoxybenzene-3-sulfonic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH169242A (en) |
-
1932
- 1932-11-15 CH CH169242D patent/CH169242A/en unknown
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